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Artificial intelligence in cosmetic dermatology 美容皮肤科中的人工智能。
IF 2.3 4区 医学 Q2 DERMATOLOGY Pub Date : 2024-08-27 DOI: 10.1111/jocd.16538
Barbara Kania BA, Karen Montecinos BS, David J. Goldberg MD

Background

Cosmetic dermatology is a growing field as more patients are seeking treatments for esthetic concerns. Traditionally, practitioners and patients utilize their own perceptions, current beauty standards, and manual observation to determine their satisfaction with cosmetic interventions. Artificial intelligence (AI) can be introduced into cosmetic dermatology to provide objective data-driven recommendations to both dermatologists and patients.

Objective

The purpose of this paper is to compose a unified review that illustrates the various facets of artificial intelligence and formulate a hypothesis regarding the new implications of artificial intelligence in cosmetic dermatology specifically.

Methods

A comprehensive search on PubMed was conducted to identify the available information related to AI in cosmetic dermatology. The search was conducted using a combination of keywords including “cosmetic dermatology” and “artificial intelligence.”

Results

The current literature indicates that AI models offer personalized, efficient, and result-driven outputs that can enhance cosmetic outcomes, patient satisfaction, and overall experience.

Conclusion

Artificial intelligence integration in cosmetic dermatology shows a promising future, offering the ability to analyze vast data sets and deliver a tailored patient experience. By incorporating AI into cosmetic dermatology, there is an opportunity to balance evidence-based decision-making with the artistic human touch of cosmetic dermatologists.

背景:随着越来越多的患者寻求美容治疗,美容皮肤科成为一个不断发展的领域。传统上,从业人员和患者利用自己的感知、当前的美容标准和人工观察来确定他们对美容干预的满意度。人工智能(AI)可被引入美容皮肤科,为皮肤科医生和患者提供客观的数据驱动型建议:本文旨在撰写一篇统一的综述,阐述人工智能的方方面面,并就人工智能在美容皮肤科领域的新影响提出假设:方法:在PubMed上进行了全面搜索,以确定与人工智能在美容皮肤科中的应用相关的可用信息。搜索使用的关键词包括 "美容皮肤科 "和 "人工智能":目前的文献表明,人工智能模型可提供个性化、高效和结果驱动的输出,从而提高美容效果、患者满意度和整体体验:结论:将人工智能融入美容皮肤科前景广阔,它能够分析大量数据集,为患者提供量身定制的体验。通过将人工智能融入美容皮肤科,有机会在循证决策与美容皮肤科医生的艺术人文关怀之间取得平衡。
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引用次数: 0
Comparison of the efficacy and safety of a 730-nm picosecond titanium sapphire laser and a 1064-nm picosecond neodymium yttrium aluminum garnet laser for the treatment of acquired bilateral nevus of Ota-like macules: A split-face, evaluator-blinded, randomized, and controlled pilot trial. 比较 730 纳米皮秒钛蓝宝石激光和 1064 纳米皮秒钕钇铝石榴石激光治疗获得性双侧太田痣样黄斑的有效性和安全性:分面、评价者盲法、随机对照试验。
IF 2.3 4区 医学 Q2 DERMATOLOGY Pub Date : 2024-08-24 DOI: 10.1111/jocd.16511
Wanxin Chen, Zhongshuai Wang, Zhenzhen Li, Chen Yuan, Xiaofeng Zhang, Li Li, Yan Yan, Baoxi Wang

Background: The picosecond neodymium yttrium aluminum garnet laser (PNYL) has been successfully used in treating acquired bilateral nevus of Ota-like macules (ABNOM). The 730-nm picosecond titanium sapphire laser (PTSL) is an emerging tool for pigmentary disorders. However, no studies have compared two different wavelengths of picosecond laser for the treatment of ABNOM.

Aims: To compare the efficacy and safety of the 730-nm PTSL with the 1064-nm PNYL in the treatment of ABNOM.

Methods: Fifteen participants with ABNOM were randomized to undergo a single session of either the 730-nm PTSL on one side of the face and 1064-nm PNYL on the other side. Efficacy and safety assessments were performed by blinded visual evaluations at baseline, 12 weeks, and 24 weeks posttreatment. Participants' satisfaction and adverse effects were recorded.

Results: Compared to baseline, The 730-nm PTSL-treated side showed better improvement than that of the 1064-nm PNYL-treated side at 24 weeks posttreatment (1.67 ± 1.047 vs. 0.87 ± 0.640, p = 0.027). There were no significant differences in pain sensation and participants' satisfaction between the two laser treatments.

Conclusions: The 730-nm PTSL is more effective than the 1064-nm PNYL in the treatment of ABNOM.

背景:皮秒钕钇铝石榴石激光(PNYL)已成功用于治疗获得性双侧太田痣样黄斑(ABNOM)。730 纳米皮秒钛蓝宝石激光器(PTSL)是治疗色素性疾病的新兴工具。目的:比较 730 波长皮秒激光和 1064 波长皮秒激光治疗 ABNOM 的有效性和安全性:方法:15 位 ABNOM 患者被随机分配到一侧面部接受 730 纳米 PTSL 治疗,另一侧接受 1064 纳米 PNYL 治疗。疗效和安全性评估分别在基线、治疗后 12 周和 24 周通过盲法视觉评估进行。参与者的满意度和不良反应也被记录在案:与基线相比,730 nm PTSL 治疗侧在治疗后 24 周的改善效果优于 1064 nm PNYL 治疗侧(1.67 ± 1.047 vs. 0.87 ± 0.640,p = 0.027)。两种激光疗法在疼痛感觉和参与者满意度方面没有明显差异:结论:在治疗 ABNOM 方面,730 波长 PTSL 比 1064 波长 PNYL 更有效。
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引用次数: 0
Efficacy and safety of non-cross-linked hyaluronic acid compound in the treatment of keratosis pilaris: A split-body randomized clinical trial. 非交联透明质酸复合物治疗毛囊角化症的有效性和安全性:分体随机临床试验。
IF 2.3 4区 医学 Q2 DERMATOLOGY Pub Date : 2024-08-23 DOI: 10.1111/jocd.16532
Yao Li, Shi-Wei Wang, Yan-Hua Liu, Mu-Yan Zou, Jia-Xu Wu, Sheng-Kang Luo, Wei-Jin Hong

Background: Keratosis pilaris (KP) is a prevalent benign dermatological condition characterized by small bumps at the hair follicles alongside surrounding redness, significantly impacting both aesthetics and mental well-being.

Objective: This study investigated the potential benefits of a non-cross-linked hyaluronic acid (HA) compound for treating KP.

Methods: A split-body, investigator-blinded, randomized, intraindividual comparative clinical trial was conducted. The non-cross-linked HA compound was injected into KP-affected regions on both upper arms. The treatment was delivered across four sessions scheduled at 4-week intervals. Blinded physicians and patients assessed differences in erythema, skin roughness, and overall scores between treated and control areas at the final follow-up visit. At the 12th and 24th weeks post-treatment, a four-point scale was utilized to assess subjects' perceived treatment efficacy. Additionally, dermoscopic images, histological alterations, and adverse events were monitored.

Results: Physician assessments revealed a significant reduction in roughness and overall scores for treated areas compared to controls. Patient self-assessments also reflected improvements in roughness, redness, and overall scores for treated sides at the final visit, with 35.71% of patients demonstrating sustained improvement in redness and 71.43% reporting persistent improvements in roughness at 24th weeks post-treatment. The dermatoscopic examinations revealed a notable enhancement in both the quantity of follicular plugs and the extent of erythema among the subjects in the treatment group. Histopathological outcomes also demonstrated improvement.

Conclusion: This study suggests that the non-cross-linked HA compound effectively improves skin roughness and promotes hair shaft growth in KP treatment, demonstrating a favorable safety profile. These findings position it as a potentially viable alternative therapy in clinical practice.

背景:毛囊角化症(Keratosis pilaris,KP)是一种常见的良性皮肤病,其特点是毛囊上长小疙瘩,周围发红,严重影响美观和心理健康:本研究调查了非交联透明质酸(HA)复合物治疗 KP 的潜在益处:方法:进行了一项分体、研究者盲法、随机、个体内比较临床试验。将非交联透明质酸化合物注射到双上臂受 KP 影响的区域。治疗分四次进行,每次间隔 4 周。双盲医生和患者在最后随访时评估治疗区和对照区在红斑、皮肤粗糙度和总体评分方面的差异。在治疗后的第 12 周和第 24 周,采用四点量表评估受试者的治疗效果。此外,还对皮肤镜图像、组织学改变和不良反应进行了监测:结果:医生的评估显示,与对照组相比,治疗部位的粗糙度和总分都有明显降低。患者的自我评估也显示,在最后一次就诊时,治疗部位的粗糙度、发红程度和总分都有所改善,35.71%的患者显示发红程度持续改善,71.43%的患者报告治疗后 24 周粗糙度持续改善。皮肤镜检查显示,治疗组受试者的毛囊栓数量和红斑程度都有明显改善。组织病理学结果也表明,治疗效果有所改善:本研究表明,非交联的 HA 复合物能有效改善皮肤粗糙度,促进 KP 治疗中的毛干生长,并显示出良好的安全性。这些发现使其成为临床实践中一种潜在的可行替代疗法。
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引用次数: 0
“Effectiveness of minimally invasive injectable modalities in the management of androgenetic alopecia among adults—A systematic review” "微创注射治疗成人雄激素性脱发的效果--系统综述》。
IF 2.3 4区 医学 Q2 DERMATOLOGY Pub Date : 2024-08-23 DOI: 10.1111/jocd.16493
Vaibhav Kumar MDS, FRSPH, Michael Gold MD, FAAD, Anuj Jain MDS, Pranjal Mhatre BDS, Ungku Mohd Shahrin b Mohd Zaman MD, M.Ed., Rinky Kapoor MD, Debraj Shome MD, FRCS (Glasgow), FACS, MBA

Background

Androgenetic alopecia is the most common cause of hair loss that affects over 50% of the world population. It is a condition that is multifactorial in origin, with no specific causative factor, making treatment an enervating experience for the patient as well as the doctor. In recent times, a number of modalities have been introduced for the treatment of alopecia. However, the evidence supporting them is unstructured and sparse. Therefore, this article aims to explore the current trends in minimally invasive treatments for the management of androgenetic alopecia.

Methods

An in-depth literature search on injectables used in the treatment of alopecia in PubMed/MEDLINE, Embase, PsycINFO, TRIP Cochrane Library, and Cochrane Skin databases between January 2000 and May 2023 was performed. The studies included were randomized controlled trials, non-randomized trials, quasi trials, single arm interventions, and cohort studies.

Results

Sixteen of the 1071 studies that were found during the original search were accepted in accordance with the inclusion criteria. Twelve studies assessed the effectiveness of the injectable group by comparing it to a control group consisting of saline, distilled water, and topical minoxidil. In the treatment of alopecia, dutasteride and injectable growth factor formulations achieved clinically significant results.

Conclusion

The usage of injectables and topical medicines to treat hair loss has increased in the recent years. Overall results from clinical investigations, pilot studies, and trials looking at the efficacy and safety of these growth factors in the AGA show satisfactory efficacy.

背景:雄激素性脱发是最常见的脱发原因,影响着全球 50%以上的人口。脱发是由多种因素引起的,没有特定的致病因素,因此治疗过程令患者和医生都感到焦虑不安。近年来,治疗脱发的方法层出不穷。然而,支持这些疗法的证据并不完整且稀少。因此,本文旨在探讨目前治疗雄激素性脱发的微创疗法的发展趋势:方法:对2000年1月至2023年5月期间PubMed/MEDLINE、Embase、PsycINFO、TRIP Cochrane Library和Cochrane Skin数据库中用于治疗脱发的注射剂进行了深入的文献检索。纳入的研究包括随机对照试验、非随机试验、准试验、单臂干预和队列研究:在最初搜索到的 1071 项研究中,有 16 项符合纳入标准。12 项研究通过将注射组与由生理盐水、蒸馏水和局部米诺地尔组成的对照组进行比较,评估了注射组的有效性。在治疗脱发方面,度他雄胺和注射生长因子制剂取得了显著的临床效果:结论:近年来,使用注射剂和外用药物治疗脱发的情况有所增加。对这些生长因子治疗 AGA 的疗效和安全性进行的临床调查、试点研究和试验的总体结果显示,疗效令人满意。
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引用次数: 0
Comparison of platelet-rich plasma efficacy with and without photoactivation in melasma: A randomized double-blind study. 比较富血小板血浆对黄褐斑的光激活与非光激活疗效:随机双盲研究
IF 2.3 4区 医学 Q2 DERMATOLOGY Pub Date : 2024-08-23 DOI: 10.1111/jocd.16540
Filiz Topaloğlu Demir, Ece Altun

Background: Photoactivation has been suggested to enhance the efficacy of platelet-rich plasma (PRP) in conditions other than dermatological diseases.

Aims: To evaluate the efficacy of photoactivated PRP (P-PRP) treatment for melasma by comparing it with non-photoactivated, classical PRP (C-PRP).

Methods: The study consisted of 38 female patients diagnosed with melasma between April 2022 and May 2023. The patients were randomized into the P-PRP and C-PRP groups. Three sessions of P-PRP or C-PRP were applied to the patients at 2-week intervals. The Melasma Area and Severity Index (MASI) and Melasma Quality of Life Index (MELASQoL) scores were compared before and 2 weeks after treatment.

Results: The median age was 38 years, and the median disease duration was 60 months. Clinically, 94.7% of the cases were centrofacial and 5.3% were malar. According to Wood's lamp examination, 55.3% of the cases were epidermal, 13.2% were dermal, and 31.6% were mixed-type. The median pre- and post-treatment scores were 14.5 and 9, respectively, for MASI and 36.5 and 17, respectively, for MELASQoL. The post-treatment MASI and MELASQoL scores of both groups significantly decreased (p < 0.001 for both). However, the intergroup difference was not significant. When all patients were evaluated together a moderate, positive, and significant relationship was detected between PRP and the pre- and post-treatment MASI and MELASQoL scores (r = 0.494 and p = 0.002). No side effects associated with PRP were observed.

Conclusion: PRP is an effective and safe treatment method for melasma. Further studies are needed to evaluate the contribution of photoactivation to PRP treatment in melasma.

背景:目的:通过与未经光激活的传统PRP(C-PRP)进行比较,评估光激活PRP(P-PRP)治疗黄褐斑的疗效:研究对象为2022年4月至2023年5月期间确诊为黄褐斑的38名女性患者。这些患者被随机分为P-PRP组和C-PRP组。每两周对患者进行三次P-PRP或C-PRP治疗。比较治疗前和治疗后两周的黄褐斑面积和严重程度指数(MASI)和黄褐斑生活质量指数(MELASQoL)得分:中位年龄为 38 岁,中位病程为 60 个月。临床上,94.7%的病例为中心面部,5.3%为颊部。伍德灯检查显示,55.3%的病例为表皮型,13.2%为真皮型,31.6%为混合型。治疗前和治疗后的 MASI 中位数分别为 14.5 分和 9 分,MELASQoL 中位数分别为 36.5 分和 17 分。两组患者治疗后的 MASI 和 MELASQoL 评分均显著下降(p 结论:PRP 是一种有效、安全的治疗方法:PRP 是一种有效、安全的黄褐斑治疗方法。还需要进一步的研究来评估光激活对 PRP 治疗黄褐斑的贡献。
{"title":"Comparison of platelet-rich plasma efficacy with and without photoactivation in melasma: A randomized double-blind study.","authors":"Filiz Topaloğlu Demir, Ece Altun","doi":"10.1111/jocd.16540","DOIUrl":"https://doi.org/10.1111/jocd.16540","url":null,"abstract":"<p><strong>Background: </strong>Photoactivation has been suggested to enhance the efficacy of platelet-rich plasma (PRP) in conditions other than dermatological diseases.</p><p><strong>Aims: </strong>To evaluate the efficacy of photoactivated PRP (P-PRP) treatment for melasma by comparing it with non-photoactivated, classical PRP (C-PRP).</p><p><strong>Methods: </strong>The study consisted of 38 female patients diagnosed with melasma between April 2022 and May 2023. The patients were randomized into the P-PRP and C-PRP groups. Three sessions of P-PRP or C-PRP were applied to the patients at 2-week intervals. The Melasma Area and Severity Index (MASI) and Melasma Quality of Life Index (MELASQoL) scores were compared before and 2 weeks after treatment.</p><p><strong>Results: </strong>The median age was 38 years, and the median disease duration was 60 months. Clinically, 94.7% of the cases were centrofacial and 5.3% were malar. According to Wood's lamp examination, 55.3% of the cases were epidermal, 13.2% were dermal, and 31.6% were mixed-type. The median pre- and post-treatment scores were 14.5 and 9, respectively, for MASI and 36.5 and 17, respectively, for MELASQoL. The post-treatment MASI and MELASQoL scores of both groups significantly decreased (p < 0.001 for both). However, the intergroup difference was not significant. When all patients were evaluated together a moderate, positive, and significant relationship was detected between PRP and the pre- and post-treatment MASI and MELASQoL scores (r = 0.494 and p = 0.002). No side effects associated with PRP were observed.</p><p><strong>Conclusion: </strong>PRP is an effective and safe treatment method for melasma. Further studies are needed to evaluate the contribution of photoactivation to PRP treatment in melasma.</p>","PeriodicalId":15546,"journal":{"name":"Journal of Cosmetic Dermatology","volume":null,"pages":null},"PeriodicalIF":2.3,"publicationDate":"2024-08-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142036016","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Investigating the inhibitory effects of carotenoids-fortified Helix aspersa slime on oxidative stress, collagenase and tyrosinase enzyme activities. 研究类胡萝卜素强化的Helix aspersa粘液对氧化应激、胶原酶和酪氨酸酶活性的抑制作用。
IF 2.3 4区 医学 Q2 DERMATOLOGY Pub Date : 2024-08-21 DOI: 10.1111/jocd.16455
Mohammed Alkhadhrh, Reem Issa, Lidia Kamal Al-Halaseh, Lilian Alnsour, Ahmad Alsarayreh, Yaseen Al Qaisi, Sina M Matalqah, Safwan Aladwan

Background: The investigations of snail slime and its possible biological activities have been performed recently.

Aim: This study aimed to evaluate the properties of Helix aspersa snail slime (HAS), and carotenoids-fortified slime (HASC).

Methods: Snails were fed with carrots for 10 days. Slime was collected and extracted using water. Saponins identification, antioxidant, collagenase, and tyrosinase enzyme inhibition activities, carotenoids, total phenols, and flavonoids content, were determined. UHPLC-MS/MS analysis was performed for phytochemical characterization.

Results: Saponins were detected in the HAS extract only. However, HASC was shown to contain a higher carotenoid content than HAS (29.51 ± 0.4 vs. 18.11 ± 0.2 μg/g). similarly, total phenolic and flavonoid content were higher for the the HASC extract compared to the HAS (182.3 ± 5.2 vs. 150.28 ± 3.3 mg/g equivalent to gallic acid), and (77.62 ± 1.2 vs. 14.19 ± 0.9 mg/g equivalent to quercetin). As expected, the HASC extract exhibited higher antioxidant activity compared to the HAS, using DPPH and the ABTS assays (IC50 = 7.75 ± 0.14 vs. 20.1 ± 0.4 μg/mL), and (IC50 = 7.6 ± 0.26 vs. 19.57 ± 1.4 μg/mL). UHPLC-MS/MS analysis revealed the presence of several phytocomponents of which, hexadecanoic acid and ascorbic acid, were observed in the HASC extract. Furthermore, HASC extract exhibited superior inhibitory activity compared to HAS against collagenase and tyrosinase enzymes (IC50 = 8.4 ± 1.19 vs. 15.3 ± 1.12 μg/mL) and (IC50 = 30.1 ± 0.91 vs. 35 ± 1.3 μg/mL).

Conclusion: These findings highlight the potential of HASC as a valuable ingredient in various pharmaceutical applications, due to their content of various phenolic, antioxidants, carotenoids, hexadecanoic, and ascorbic acids. The latter is well known for its great cosmeceutical applications used for slowing the process of skin aging.

背景:最近对蜗牛粘液及其可能的生物活性进行了研究:目的:本研究旨在评估 Helix aspersa 蜗牛粘液(HAS)和类胡萝卜素强化粘液(HASC)的特性:方法:用胡萝卜喂养蜗牛10天。方法:用胡萝卜喂养蜗牛 10 天,收集粘液并用水提取。测定皂甙鉴定、抗氧化剂、胶原酶和酪氨酸酶抑制活性、类胡萝卜素、总酚和类黄酮含量。对植物化学特征进行了超高效液相色谱-质谱/质谱分析:结果:仅在 HAS 提取物中检测到皂苷。同样,与 HAS 相比,HASC 提取物的总酚和类黄酮含量更高(182.3 ± 5.2 vs. 150.28 ± 3.3 mg/g,相当于没食子酸)和(77.62 ± 1.2 vs. 14.19 ± 0.9 mg/g,相当于槲皮素)。正如预期的那样,与 HAS 相比,HASC 提取物在 DPPH 和 ABTS 试验中表现出更高的抗氧化活性(IC50 = 7.75 ± 0.14 vs. 20.1 ± 0.4 μg/mL)和(IC50 = 7.6 ± 0.26 vs. 19.57 ± 1.4 μg/mL)。超高效液相色谱-质谱-质谱分析表明,HASC 提取物中含有多种植物成分,其中包括十六烷酸和抗坏血酸。此外,HASC 提取物对胶原酶和酪氨酸酶(IC50 = 8.4 ± 1.19 vs. 15.3 ± 1.12 μg/mL)和(IC50 = 30.1 ± 0.91 vs. 35 ± 1.3 μg/mL)的抑制活性优于 HAS:这些发现凸显了 HASC 作为各种药物应用中的重要成分的潜力,因为它们含有各种酚类、抗氧化剂、类胡萝卜素、十六烷酸和抗坏血酸。其中,抗坏血酸因其在减缓皮肤衰老方面的巨大药用价值而闻名。
{"title":"Investigating the inhibitory effects of carotenoids-fortified Helix aspersa slime on oxidative stress, collagenase and tyrosinase enzyme activities.","authors":"Mohammed Alkhadhrh, Reem Issa, Lidia Kamal Al-Halaseh, Lilian Alnsour, Ahmad Alsarayreh, Yaseen Al Qaisi, Sina M Matalqah, Safwan Aladwan","doi":"10.1111/jocd.16455","DOIUrl":"https://doi.org/10.1111/jocd.16455","url":null,"abstract":"<p><strong>Background: </strong>The investigations of snail slime and its possible biological activities have been performed recently.</p><p><strong>Aim: </strong>This study aimed to evaluate the properties of Helix aspersa snail slime (HAS), and carotenoids-fortified slime (HASC).</p><p><strong>Methods: </strong>Snails were fed with carrots for 10 days. Slime was collected and extracted using water. Saponins identification, antioxidant, collagenase, and tyrosinase enzyme inhibition activities, carotenoids, total phenols, and flavonoids content, were determined. UHPLC-MS/MS analysis was performed for phytochemical characterization.</p><p><strong>Results: </strong>Saponins were detected in the HAS extract only. However, HASC was shown to contain a higher carotenoid content than HAS (29.51 ± 0.4 vs. 18.11 ± 0.2 μg/g). similarly, total phenolic and flavonoid content were higher for the the HASC extract compared to the HAS (182.3 ± 5.2 vs. 150.28 ± 3.3 mg/g equivalent to gallic acid), and (77.62 ± 1.2 vs. 14.19 ± 0.9 mg/g equivalent to quercetin). As expected, the HASC extract exhibited higher antioxidant activity compared to the HAS, using DPPH and the ABTS assays (IC<sub>50</sub> = 7.75 ± 0.14 vs. 20.1 ± 0.4 μg/mL), and (IC<sub>50</sub> = 7.6 ± 0.26 vs. 19.57 ± 1.4 μg/mL). UHPLC-MS/MS analysis revealed the presence of several phytocomponents of which, hexadecanoic acid and ascorbic acid, were observed in the HASC extract. Furthermore, HASC extract exhibited superior inhibitory activity compared to HAS against collagenase and tyrosinase enzymes (IC<sub>50</sub> = 8.4 ± 1.19 vs. 15.3 ± 1.12 μg/mL) and (IC<sub>50</sub> = 30.1 ± 0.91 vs. 35 ± 1.3 μg/mL).</p><p><strong>Conclusion: </strong>These findings highlight the potential of HASC as a valuable ingredient in various pharmaceutical applications, due to their content of various phenolic, antioxidants, carotenoids, hexadecanoic, and ascorbic acids. The latter is well known for its great cosmeceutical applications used for slowing the process of skin aging.</p>","PeriodicalId":15546,"journal":{"name":"Journal of Cosmetic Dermatology","volume":null,"pages":null},"PeriodicalIF":2.3,"publicationDate":"2024-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142017682","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Novel injectable polypeptide nanoparticle encapsulated siRNA targeting TGF-β1 and COX-2 for localized fat reduction I: Preclinical in vitro and animal models 针对 TGF-β1 和 COX-2 的新型可注射多肽纳米粒子包裹 siRNA 用于局部减脂 I:临床前体外和动物模型。
IF 2.3 4区 医学 Q2 DERMATOLOGY Pub Date : 2024-08-21 DOI: 10.1111/jocd.16535
Mark S. Nestor MD, PhD, John Hetzel MD, Nardin Awad DO, Vishnu Bhupalam BS, Patrick Lu PhD, Michael Molyneaux MD

Background

Obesity and localized fat accumulation continue to drive the demand for minimally invasive body contouring technologies including injectable compounds for local fat reduction. siRNA offers a potential for an injectable to specifically target and silence genes involved in adipogenesis with minimal inflammatory side effects.

Aims

This study evaluates the efficacy of STP705, an injectable containing siRNA encapsulated within histidine-lysine polypeptide (HKP) nanoparticles targeting transforming growth factor β1 (TGF-β1) and cyclooxygenase-2 (COX-2), crucial mediators in adipocyte differentiation and fat retention, using in vitro, porcine, and murine models.

Methods

In vitro experiments on mouse preadipocytes and in vivo trials using Diet Induced Obese (DIO) mice and Yucatan minipigs were conducted to assess the gene silencing efficiency, tissue localization, pharmacodynamics, and safety profile of STP705.

Results

STP705 effectively reduced the expression of TGF-β1 and COX-2, with a notable decrease in adipocyte volume and lipid content without adverse systemic effects. In DIO mice, the HKP-siRNA complex demonstrated precise localization to injected adipose tissue, maintaining significant gene silencing, and detectable levels of siRNA for up to 14 days post-administration. Similar results in minipigs showed a significant reduction in subcutaneous adipose tissue thickness.

Conclusion

The results of these studies support the use of targeted siRNA therapy specifically targeting TGF-β1 and COX-2, for localized fat reduction, offering a potential minimally invasive alternative to current fat reduction methods.

背景:siRNA 为注射剂提供了一种潜力,它能特异性地靶向并沉默参与脂肪生成的基因,同时将炎症副作用降到最低。目的:本研究利用体外、猪和小鼠模型评估了含有 siRNA 的注射剂 STP705 的疗效,这种 siRNA 封装在组氨酸-赖氨酸多肽(HKP)纳米颗粒中,靶向转化生长因子 β1 (TGF-β1) 和环氧化酶-2 (COX-2),它们是脂肪细胞分化和脂肪滞留的关键介质:方法:对小鼠前脂肪细胞进行体外实验,并使用饮食诱导肥胖(DIO)小鼠和尤卡坦小猪进行体内试验,以评估 STP705 的基因沉默效率、组织定位、药效学和安全性:结果:STP705能有效降低TGF-β1和COX-2的表达,显著减少脂肪细胞体积和脂质含量,且不会对全身产生不良影响。在 DIO 小鼠中,HKP-siRNA 复合物显示出精确定位到注射的脂肪组织,保持了显著的基因沉默,并在给药后长达 14 天的时间里仍能检测到 siRNA 的水平。在迷你猪身上的类似结果表明,皮下脂肪组织厚度明显减少:这些研究结果支持使用专门针对 TGF-β1 和 COX-2 的靶向 siRNA 疗法进行局部减脂,为目前的减脂方法提供了一种潜在的微创替代方法。
{"title":"Novel injectable polypeptide nanoparticle encapsulated siRNA targeting TGF-β1 and COX-2 for localized fat reduction I: Preclinical in vitro and animal models","authors":"Mark S. Nestor MD, PhD,&nbsp;John Hetzel MD,&nbsp;Nardin Awad DO,&nbsp;Vishnu Bhupalam BS,&nbsp;Patrick Lu PhD,&nbsp;Michael Molyneaux MD","doi":"10.1111/jocd.16535","DOIUrl":"10.1111/jocd.16535","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Background</h3>\u0000 \u0000 <p>Obesity and localized fat accumulation continue to drive the demand for minimally invasive body contouring technologies including injectable compounds for local fat reduction. siRNA offers a potential for an injectable to specifically target and silence genes involved in adipogenesis with minimal inflammatory side effects.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Aims</h3>\u0000 \u0000 <p>This study evaluates the efficacy of STP705, an injectable containing siRNA encapsulated within histidine-lysine polypeptide (HKP) nanoparticles targeting transforming growth factor β1 (TGF-β1) and cyclooxygenase-2 (COX-2), crucial mediators in adipocyte differentiation and fat retention, using in vitro, porcine, and murine models.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>In vitro experiments on mouse preadipocytes and in vivo trials using Diet Induced Obese (DIO) mice and Yucatan minipigs were conducted to assess the gene silencing efficiency, tissue localization, pharmacodynamics, and safety profile of STP705.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>STP705 effectively reduced the expression of TGF-β1 and COX-2, with a notable decrease in adipocyte volume and lipid content without adverse systemic effects. In DIO mice, the HKP-siRNA complex demonstrated precise localization to injected adipose tissue, maintaining significant gene silencing, and detectable levels of siRNA for up to 14 days post-administration. Similar results in minipigs showed a significant reduction in subcutaneous adipose tissue thickness.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>The results of these studies support the use of targeted siRNA therapy specifically targeting TGF-β1 and COX-2, for localized fat reduction, offering a potential minimally invasive alternative to current fat reduction methods.</p>\u0000 </section>\u0000 </div>","PeriodicalId":15546,"journal":{"name":"Journal of Cosmetic Dermatology","volume":null,"pages":null},"PeriodicalIF":2.3,"publicationDate":"2024-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jocd.16535","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142017632","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Evaluation of the safety and efficacy of concentrated growth factors for hair growth promotion in androgenetic alopecia patients: A retrospective single-centre, single-arm study. 评估浓缩生长因子促进雄激素性脱发患者毛发生长的安全性和有效性:单中心、单臂回顾性研究。
IF 2.3 4区 医学 Q2 DERMATOLOGY Pub Date : 2024-08-21 DOI: 10.1111/jocd.16519
Saisai Cao, Mengyi Zhu, Ye Bi

Objective: This study was designed to evaluate the safety and efficacy of injections of concentrated growth factors (CGF) for hair growth promotion in androgenetic alopecia (AGA) patients.

Methods: A retrospective review of AGA patients treated with injections of CGF at our center from October 2021 to April 2023 was performed. A total of 3 injections were administered every 3-4 weeks apart, and evaluation were performed before the first injection and at 3 months, 6 months later. The outcomes were assessed by trichoscopy photomicrographs and the Global Aesthetic Improvement Scale (GAIS).

Results: At 3 months after the first injection, the hair density and hair growth ratio were significantly improved. Significant improvements were found in GAIS score by both patients and independent doctors and the hair growth promotion was sustained for 6 months after first treatment.

Conclusions: According to this tiny single-arm trial, the use of CGF injection may help AGA by increasing terminal hair density and hair density. No severe topical or systemic adverse events occurred during the treatment.

研究目的本研究旨在评估注射浓缩生长因子(CGF)促进雄激素性脱发(AGA)患者毛发生长的安全性和有效性:对2021年10月至2023年4月期间在本中心接受CGF注射治疗的AGA患者进行回顾性研究。每隔3-4周注射一次,共注射3次,在首次注射前、3个月后和6个月后进行评估。结果通过三镜显微照片和全球美学改善量表(GAIS)进行评估:结果:首次注射后 3 个月,毛发密度和毛发生长比例均有明显改善。结果:首次注射后 3 个月,毛发密度和毛发生长比例均有明显改善,患者和独立医生的 GAIS 评分均有明显改善,毛发生长促进作用在首次治疗后持续了 6 个月:结论:根据这项微小的单臂试验,CGF注射液可通过增加末端毛发密度和毛发密度来帮助AGA。治疗期间未发生严重的局部或全身不良反应。
{"title":"Evaluation of the safety and efficacy of concentrated growth factors for hair growth promotion in androgenetic alopecia patients: A retrospective single-centre, single-arm study.","authors":"Saisai Cao, Mengyi Zhu, Ye Bi","doi":"10.1111/jocd.16519","DOIUrl":"https://doi.org/10.1111/jocd.16519","url":null,"abstract":"<p><strong>Objective: </strong>This study was designed to evaluate the safety and efficacy of injections of concentrated growth factors (CGF) for hair growth promotion in androgenetic alopecia (AGA) patients.</p><p><strong>Methods: </strong>A retrospective review of AGA patients treated with injections of CGF at our center from October 2021 to April 2023 was performed. A total of 3 injections were administered every 3-4 weeks apart, and evaluation were performed before the first injection and at 3 months, 6 months later. The outcomes were assessed by trichoscopy photomicrographs and the Global Aesthetic Improvement Scale (GAIS).</p><p><strong>Results: </strong>At 3 months after the first injection, the hair density and hair growth ratio were significantly improved. Significant improvements were found in GAIS score by both patients and independent doctors and the hair growth promotion was sustained for 6 months after first treatment.</p><p><strong>Conclusions: </strong>According to this tiny single-arm trial, the use of CGF injection may help AGA by increasing terminal hair density and hair density. No severe topical or systemic adverse events occurred during the treatment.</p>","PeriodicalId":15546,"journal":{"name":"Journal of Cosmetic Dermatology","volume":null,"pages":null},"PeriodicalIF":2.3,"publicationDate":"2024-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142017681","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
An in vivo approach for revealing physiological properties of human scalp microbiome. 揭示人类头皮微生物群生理特性的体内方法。
IF 2.3 4区 医学 Q2 DERMATOLOGY Pub Date : 2024-08-21 DOI: 10.1111/jocd.16524
Jang Ho Joo, Jaeyoon Kim, Jae Young Shin, Yun-Ho Choi, Seung-Hyun Jun, Nae-Gyu Kang
{"title":"An in vivo approach for revealing physiological properties of human scalp microbiome.","authors":"Jang Ho Joo, Jaeyoon Kim, Jae Young Shin, Yun-Ho Choi, Seung-Hyun Jun, Nae-Gyu Kang","doi":"10.1111/jocd.16524","DOIUrl":"https://doi.org/10.1111/jocd.16524","url":null,"abstract":"","PeriodicalId":15546,"journal":{"name":"Journal of Cosmetic Dermatology","volume":null,"pages":null},"PeriodicalIF":2.3,"publicationDate":"2024-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142017680","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Krill oil supplementation improves transepidermal water loss, hydration and elasticity of the skin in healthy adults: Results from two randomized, double-blind, placebo-controlled, dose-finding pilot studies. 补充磷虾油能改善健康成年人的经表皮失水、皮肤水合作用和弹性:两项随机、双盲、安慰剂对照、剂量试验研究的结果。
IF 2.3 4区 医学 Q2 DERMATOLOGY Pub Date : 2024-08-21 DOI: 10.1111/jocd.16513
Katina Handeland, Mike Wakeman, Lena Burri

Background: Dietary marine omega-3 fatty acids and phospholipids have individually shown favorable effects on skin barrier function. Krill oil offers a combination of omega-3 in phospholipid form which might enhance the efficacy in supporting skin health.

Aims: The aim was to investigate the impact of two different doses of krill oil on skin transepidermal water loss (TEWL) in healthy adults. Secondary outcomes were skin hydration, elasticity and the omega-3 index.

Methods: Two randomized, double-blind, placebo-controlled, pilot studies were conducted in healthy adults with a baseline TEWL of >10 and ≤24.9 g/m2/h. In study 1, 51 participants consumed 1 g of krill oil or placebo daily. In study 2, 50 participants consumed 2 g of krill oil or placebo daily. The outcomes were assessed at baseline, 6 and 12 weeks.

Results: The krill oil supplemented groups significantly increased their omega-3 index versus placebo in both studies. Furthermore, the krill oil groups in both studies showed statistically significant beneficial reductions in TEWL (from 14.47 ± 3.65 to 13.83 ± 3.78 in study 1 and from 14.25 ± 3.21 to 13.02 ± 2.76 in study 2) and increases in hydration and elasticity when compared to placebo. There were significant linear relationships between changes in the omega-3 index and changes in TEWL, hydration and elasticity in both studies.

Conclusions: Daily oral supplementation with 1 and 2 g of krill oil showed significant and dose-dependent improvements in skin TEWL, hydration, and elasticity compared to placebo that correlated with changes in the omega-3 index.

背景:膳食中的海洋ω-3脂肪酸和磷脂已分别显示出对皮肤屏障功能的有利影响。磷虾油提供了磷脂形式的欧米加-3组合,可能会增强支持皮肤健康的功效。目的:研究旨在调查两种不同剂量的磷虾油对健康成年人皮肤经表皮失水(TEWL)的影响。次要结果是皮肤水合作用、弹性和欧米茄-3 指数:在基线 TEWL >10 和 ≤24.9 g/m2/h 的健康成年人中进行了两项随机、双盲、安慰剂对照试验研究。在研究 1 中,51 名参与者每天食用 1 克磷虾油或安慰剂。在研究 2 中,50 名参与者每天摄入 2 克磷虾油或安慰剂。结果在基线、6 周和 12 周时进行了评估:结果:在这两项研究中,磷虾油补充组与安慰剂组相比,ω-3指数都有显著提高。此外,与安慰剂相比,两项研究中磷虾油组的 TEWL(从 14.47 ± 3.65 降至 13.83 ± 3.78,见研究 1;从 14.25 ± 3.21 降至 13.02 ± 2.76,见研究 2)均有统计学意义的显著降低,水合作用和弹性也有增加。在两项研究中,欧米伽-3指数的变化与TEWL、水合作用和弹性的变化之间存在明显的线性关系:结论:与安慰剂相比,每天口服 1 克和 2 克磷虾油可显著改善皮肤 TEWL、水合作用和弹性,且与欧米伽-3 指数的变化相关,且呈剂量依赖性。
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引用次数: 0
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Journal of Cosmetic Dermatology
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